Chapter 9: Problem 16
What property of the electron causes electron domains to have an effect on molecular shapes?
Chapter 9: Problem 16
What property of the electron causes electron domains to have an effect on molecular shapes?
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Get started for freeButadiene, \(\mathrm{C}_{4} \mathrm{H}_{6}\) is a planar molecule that has the following carbocarbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle \(C-\) bond length in butadiene \((1.48\) A) is a little shorter than the average \(\mathrm{C}-\mathrm{C}\) single bond length \((1.54 \hat{\mathrm{A}}) .\) Does this imply that the middle \(\mathrm{C}-\mathrm{Cbond}\) in butadiene is weaker or stronger than the average \(\mathrm{C}-\mathrm{C}\)? (\mathbf{d} ) Based on your answer for part ( c ),discuss what additional aspects of bonding in butadiene might support the shorter middle \(\mathrm{C}-\) C bond.
The reaction of three molecules of fluorine gas with a Xe atom produces the substance xenon hexafluoride, \(\mathrm{XeF}_{6}\) : $$\mathrm{Xe}(g)+3 \mathrm{~F}_{2}(g) \longrightarrow \mathrm{XeF}_{6}(s) $$ (a) Draw a Lewis structure for \(\mathrm{XeF}_{6}\). (b) If you try to use the VSEPR model to predict the molecular geometry of \(\mathrm{XeF}_{6}\), you run into a problem. What is it? (c) What could you do to resolve the difficulty in part \((\mathrm{b}) ?(\mathbf{d})\) The molecule \(\mathrm{IF}_{7}\) has a pentagonalbipyramidal structure (five equatorial fluorine atoms at the vertices of a regular pentagon and two axial fluorine atoms). Based on the structure of \(\mathrm{IF}_{7}\), suggest a structure for \(\mathrm{XeF}_{6}\).
(a) Starting with the orbital diagram of a boron atom, describe the steps needed to construct hybrid orbitals appropriate to describe the bonding in \(\mathrm{BF}_{3}\). (b) What is the name given to the hybrid orbitals constructed in (a)? (c) Sketch the large lobes of the hybrid orbitals constructed in part (a). (d) Are any valence atomic orbitals of \(\mathrm{B}\) left unhybridized? If so, how are they oriented relative to the hybrid orbitals?
(a) Write a single Lewis structure for \(\mathrm{SO}_{3}\), and determine the hybridization at the \(\mathrm{S}\) atom. (b) Are there other equivalent Lewis structures for the molecule? (c) Would you expect \(\mathrm{SO}_{3}\) to exhibit delocalized \(\pi\) bonding? Explain.
In ozone, \(\mathrm{O}_{3},\) the two oxygen atoms on the ends of the molecule are equivalent to one another. (a) What is the best choice of hybridization scheme for the atoms of ozone? (b) For one of the resonance forms of ozone, which of the orbitals are used to make bonds and which are used to hold nonbonding pairs of electrons? (c) Which of the orbitals can be used to delocalize the \(\pi\) electrons? (d) How many electrons are delocalized in the \(\pi\) system of ozone?
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